Elf Buff Acne Fighting Foundation label

Elf Buff Acne Fighting Foundation

Elf Buff Acne Fighting Foundation Recall

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Side Effects & Adverse Reactions

There is currently no side effect or adverse reaction information available for this drug.

FDA Safety Alerts

There are currently no FDA safety alerts available for this drug.

Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.

Uses

There is current no usage information for this drug.

History

There is currently no drug history available for this drug.

Other Information

There is currently no other information available for this drug.

Elf Buff Acne Fighting Foundation Manufacturers

  • J. A. Cosmetics U.s. Inc
    Elf Buff Acne Fighting Foundation | Remedyrepack Inc.
    No Recall

    Elf Buff Acne Fighting Foundation | Remedyrepack Inc.

    Elf Buff Acne Fighting Foundation | Remedyrepack Inc.

    A single intramuscular injection of 0.5 mL. (2.1)

     

    Just before use, shake the vial or syringe well until a uniform, white, cloudy suspension results.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. If either of these conditions exist, the vaccine should not be administered.

    When withdrawing a dose from a stoppered vial, do not remove either the stopper or the metal seal holding it in place. Use a separate sterile needle and syringe for each injection. Using a sterile needle and syringe, withdraw the 0.5 mL dose of vaccine from the single-dose vial and administer the vaccine to the individual. Changing needles between withdrawing the vaccine from the vial and injecting it into a recipient is not necessary unless the needle has been damaged or contaminated.

    Adacel vaccine should not be combined through reconstitution or mixed with any other vaccine.

     

    Adacel vaccine is administered as a single 0.5 mL intramuscular injection into the deltoid muscle of the upper arm.

    Do not administer this product intravenously, subcutaneously or intradermally.

    There are no data to support repeat administration of Adacel vaccine.

    Five years should have elapsed since the recipient's last dose of tetanus toxoid, diphtheria toxoid and/or pertussis containing vaccine and the administration of Adacel vaccine.

     

    Primary series: The safety and effectiveness of Adacel vaccine used as a primary series or to complete the primary series, for diphtheria, tetanus, or pertussis has not been demonstrated.

     

    Wound management: If tetanus prophylaxis is needed for wound management, Adacel may be given if no previous dose of any Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Adsorbed (Tdap) has been administered.